| Tag | Content |
|---|
EnhancerAtlas ID | HS121-18467 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr19:1226660-1227590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr19:1227044-1227064 | TGGTGGGTGGTGGGGAGGGG | - | 6.3 | | RREB1 | MA0073.1 | chr19:1227041-1227061 | GGGTGGTGGGTGGTGGGGAG | - | 6.63 | | Stat4 | MA0518.1 | chr19:1226989-1227003 | CTTCCAGGAAAGGC | + | 6.02 | | Zfx | MA0146.2 | chr19:1227060-1227074 | GGGGCCGCGGCCTC | + | 6.59 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I001227 | chr19 | 1227316 | 1228274 |
|
Enhancer Sequence | AGGTGGGGCG CGGCGGGGCC CGGGTGGGGC ATGTGGGGAC AACGCCTGGA TGCCACAGCC 60
AGCCGTGAGC ATAGCCCGCG CTAGTCAGTC ATGGTGACCG TCACGTGGCT GCGCGTGGTT 120
GCCATGTGGC CTTTGGGTGG CTTGGCCACG TAGCGATCCC CGTGGAGGGT GCCGTCTCGG 180
GGCCTGGTGT CTGGCCAGCG TGCTGGTCAT GGAGGCCTAC GTGTGGCGGG GCTCTGGGGG 240
GGCGTGCCGT CCTCACAGCC ACCTCTCAGA GTGGGTGCAT TCCGAGGACC CTGCCCTGGG 300
CCTGGCGCCC CCTCCCCATG CCCGCGCCGC TTCCAGGAAA GGCTTATGCT GGGCTCAGCC 360
CAGAGGCTTT TGAGCACCAG TGGGTGGTGG GTGGTGGGGA GGGGCCGCGG CCTCCATGGC 420
TCTGCCGGGG TGCCGCAGGC TCTGAGCCAG CTGCCAAGTA TGGCTGAGGC TGAGTCGTGC 480
CGGACGCTGC CCTGTCTCTC CCTGTGTGCC TGCCTCCTCT CCCAGCCCCA GCCCCAGCCC 540
CGGGTGGGAG ACGGAGTCCC AGAGGTGTCA GAGACCCTTA AGTCACCTGC CGAGGATGCG 600
GGGTGGATGG GGGCCCGAGG CTGAAGCCCC TGCCTTGCCA CAGCCCCTCT CCCAGGTTTT 660
GGGGGCCACC GCCTGAGTTA CATGTCTGTC CCCCAAATGG GTGCCCACAG CCCATCCACC 720
AGCGTCAGAG CCCGCCAGGC CCCACTGCAA AAGGCCACAC AATGTACCCC GGGAGTGACT 780
CAAGGGTGGC CTTCCCTGGC CTCCCCTGCT GCCCCCCAGG AGTCCGGTAG CCCCATGACT 840
GTACCTCAGC TTCTCCATCC TCCCAGGGGC CCGCGGGAGG CGGAGAACCG GTGCCCAGGC 900
TGACCTCTTC CGTCTTCCTT CCACCCTGCA 930
|
